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Département: Institut de l’Audition – Centre de l’Institut Pasteur
Tous Publications
2024
Ghizlene Lahlou, Charlotte Calvet, François Simon, Vincent Michel, Lauranne Alciato, Baptiste Plion, Jacques Boutet de Monvel, Marie-José Lecomte, Mathieu Beraneck, Christine Petit, Saaid Safieddine,
Extended time frame for restoring inner ear function through gene therapy in Usher1G preclinical model,
JCI Insight, 2024, 9 (3), pp.e169504. ⟨10.1172/jci.insight.169504⟩.
2023
Christine Petit, Crystel Bonnet, Saaïd Safieddine,
Deafness: from genetic architecture to gene therapy,
Nature Reviews Genetics, 2023, ⟨10.1038/s41576-023-00597-7⟩.
2022
Aziz El-Amraoui, Gwenaelle G S Géléoc,
Usher syndrome Recent advances in our understanding of genes and therapeutics,
Research Outreach, 2022, 131, ⟨10.32907/RO-131-3039996892⟩.
2022
Audrey Maudoux, Sandrine Vitry, Aziz El-Amraoui,
Vestibular Deficits in Deafness: Clinical Presentation, Animal Modeling, and Treatment Solutions,
Frontiers in Neurology, 2022, 13, pp.816534. ⟨10.3389/fneur.2022.816534⟩.
2022
Sedigheh Delmaghani, Aziz El-Amraoui,
The genetic and phenotypic landscapes of Usher syndrome: from disease mechanisms to a new classification,
Human Genetics, 2022, 141 (3-4), pp.709-735. ⟨10.1007/s00439-022-02448-7⟩.
2021
Aziz El-Amraoui,
Vieillissement de l’oreille interne : bases génétiques et conséquences à l’échelle cellulaire et moléculaire.,
Le vieillissement cochléo-vestibulaire : Rapport SFORL 2021, Elsevier Masson, pp.23-34, 2021, 9782294772948.
2021
Barbara Vona, Neda Mazaheri, Sheng-Jia Lin, Lucy A Dunbar, Reza Maroofian, Hela Azaiez, Kevin T Booth, Sandrine Vitry, Aboulfazl Rad, Franz Rüschendorf, Pratishtha Varshney, Ben Fowler, Christian Beetz, Kumar N Alagramam, David Murphy, Gholamreza Shariati, Alireza Sedaghat, Henry Houlden, Cassidy Petree, Shruthi Vijaykumar, Richard J H Smith, Thomas Haaf, Aziz El-Amraoui, Michael R Bowl, Gaurav K Varshney, Hamid Galehdari,
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans,
Human Genetics, 2021, 140 (6), pp.915 - 931. ⟨10.1007/s00439-020-02254-z⟩.
2021
Eric Nisenbaum, Torin Thielhelm, Aida Nourbakhsh, Denise Yan, Susan Blanton, Yilai Shu, Karl Koehler, Aziz El-Amraoui, Zhengyi Chen, Byron Lam, Xuezhong Liu,
Review of Genotype-Phenotype Correlations in Usher Syndrome,
Ear & Hearing, 2022, 43 (1), pp.1-8. ⟨10.1097/AUD.0000000000001066⟩.
2021
Aida Nourbakhsh, Brett M. Colbert, Eric Nisenbaum, Aziz El-Amraoui, Derek M. Dykxhoorn, Karl Russell Koehler, Zheng-Yi Chen, Xue Z. Liu,
Stem Cells and Gene Therapy in Progressive Hearing Loss: the State of the Art,
Journal of the Association for Research in Otolaryngology, 2021, 22 (2), pp.95-105. ⟨10.1007/s10162-020-00781-0⟩.
2021
Catherine Botto, Deniz Dalkara, Aziz El-Amraoui,
Progress in Gene Editing Tools and Their Potential for Correcting Mutations Underlying Hearing and Vision Loss,
Frontiers in Genome Editing, 2021, 3, pp.737632. ⟨10.3389/fgeed.2021.737632⟩.
2020
Gwenaelle G S Géléoc, Aziz El-Amraoui,
Disease mechanisms and gene therapy for Usher syndrome,
Hearing Research, 2020, 394, pp.107932. ⟨10.1016/j.heares.2020.107932⟩.
2020
Sedigheh Delmaghani, Aziz El-Amraoui,
Inner Ear Gene Therapies Take Off: Current Promises and Future Challenges,
Journal of Clinical Medicine, 2020, 9 (7), pp.2309. ⟨10.3390/jcm9072309⟩.
2020
Cherine Charfeddine, Hamza Dallali, Ghaith Abdessalem, Kais Ghedira, Yosr Hamdi, Sahar Elouej, Zied Landoulsi, Valérie Delague, Arnaud Lagarde, Nicolas Levy, Aziz El-Amraoui, Mohamed Samir Boubaker, Sonia Abdelhak, Mourad Mokni,
Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family,
Journal of Human Genetics, 2020, 65 (4), pp.397 - 410. ⟨10.1038/s10038-019-0711-4⟩.
2019
Lucy A Dunbar, Pranav Patni, Carlos Aguilar, Philomena Mburu, Laura Corns, Helena Rr Wells, Sedigheh Delmaghani, Andrew Parker, Stuart Johnson, Debbie Williams, Christopher T Esapa, Michelle M Simon, Lauren Chessum, Sherylanne Newton, Joanne Dorning, Prashanthini Jeyarajan, Susan Morse, Andrea Lelli, Gemma F Codner, Thibault Peineau, Suhasini R Gopal, Kumar N Alagramam, Ronna Hertzano, Didier Dulon, Sara Wells, Frances M Williams, Christine Petit, Sally J Dawson, Steve Dm Brown, Walter Marcotti, Aziz El-Amraoui, Michael R Bowl,
Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function,
EMBO Molecular Medicine, 2019, 11 (9), pp.e10288. ⟨10.15252/emmm.201910288⟩.
2018
Aubin Samacoits, Racha Chouaib, Adham Safieddine, Abdel-Meneem Traboulsi, Christophe Zimmer, Wei Ouyang, Marion Peter, Edouard Bertrand, Thomas Walter, Florian Mueller,
A computational framework to study sub-cellular RNA localization,
Nature Communications, 2018, 9 (1), pp.4584. ⟨10.1038/s41467-018-06868-w⟩.
2018
K.T. Booth, K. Kahrizi, M. Babanejad, H. Daghagh, G. Bademci, S. Arzhangi, D. Zareabdollahi, D. Duman, A. El-Amraoui, M. Tekin, H. Najmabadi, H. Azaiez, R.J. Smith,
Variants in CIB2 cause DFNB48 and not USH1J,
Clinical Genetics, 2018, 93 (4), pp.812-821. ⟨10.1111/cge.13170⟩.
2018
Alix Trouillet, Elisabeth Dubus, Julie Degardin, Amrit Estivalet, Ivana Ivkovic, David Godefroy, Diego García-Ayuso, Manuel Simonutti, Iman Sahly, José-Alain Sahel, Aziz El-Amraoui, Christine Petit, Serge Picaud,
Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments,
Scientific Reports, 2018, 8 (1), pp.1968. ⟨10.1038/s41598-018-20171-0⟩.
2017
Vincent Michel, Kevin T Booth, Pranav Patni, Matteo Cortese, Hela Azaiez, Amel Bahloul, Kimia Kahrizi, Ménélik Labbe, Alice Emptoz, Andrea Lelli, Julie Dégardin, Typhaine Dupont, Asadollah Aghaie, Danuta Oficjalska‐pham, Serge Picaud, Hossein Najmabadi, Richard J Smith, Michael R Bowl, Steven Dm Brown, Paul Avan, Christine Petit, Aziz El‐amraoui,
CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival,
EMBO Molecular Medicine, 2017, 9 (12), pp.1711 - 1731. ⟨10.15252/emmm.201708087⟩.
2017
Amel Bahloul, Elise Pepermans, Bertrand Raynal, Nicolas Wolff, Florence Cordier, Patrick England, Sylvie Nouaille, Bruno Baron, Aziz El-Amraoui, Jean-Pierre Hardelin, Dominique Durand, Christine Petit,
Conformational switch of harmonin, a submembrane scaffold protein of the hair cell mechanoelectrical transduction machinery,
FEBS Letters, 2017, 591 (15), pp.2299 - 2310. ⟨10.1002/1873-3468.12729⟩.
2017
Cataldo Schietroma, Karine Parain, Amrit Estivalet, Asadollah Aghaie, Jacques Boutet de Monvel, Serge Picaud, José-Alain Sahel, Muriel Perron, Aziz El-Amraoui, Christine Petit,
Usher syndrome type 1–associated cadherins shape the photoreceptor outer segment,
Journal of Cell Biology, 2017, 216 (6), pp.1849 - 1864. ⟨10.1083/jcb.201612030⟩.
2017
Philippe F.Y. Vincent, Yohan Bouleau, Gilles Charpentier, Alice Emptoz, Saaid Safieddine, Christine Petit, Didier Dulon,
Different Ca V 1.3 Channel Isoforms Control Distinct Components of the Synaptic Vesicle Cycle in Auditory Inner Hair Cells,
Journal of Neuroscience, 2017, 37 (11), pp.2960-2975. ⟨10.1523/JNEUROSCI.2374-16.2017⟩.
2017
Matteo Cortese, Samantha Papal, Francisco Pisciottano, Ana Belén Elgoyhen, Jean-Pierre Hardelin, Christine Petit, Lucia Florencia Franchini, Aziz El-Amraoui,
Spectrin βV adaptive mutations and changes in subcellular location correlate with emergence of hair cell electromotility in mammalians.,
Proceedings of the National Academy of Sciences of the United States of America, 2017, 114 (8), pp.2054-2059. ⟨10.1073/pnas.1618778114⟩.
2016
Crystel Bonnet, Zied Riahi, Sandra Chantot-Bastaraud, Luce Smagghe, Mélanie Letexier, Charles Marcaillou, Gaëlle Lefèvre, Jean-Pierre Hardelin, Aziz El-Amraoui, Amrit Singh-Estivalet, Saddek Mohand-Saïd, Susanne Kohl, Anne Kurtenbach, Ieva Sliesoraityte, Ditta Zobor, Souad Gherbi, Francesco Testa, Francesca Simonelli, Sandro Banfi, Ana Fakin, Damjan Glavač, Martina Jarc-Vidmar, Andrej Zupan, Saba Battelino, Loreto Martorell Sampol, Maria Antonia Claveria, Jaume Catala Mora, Shzeena Dad, Lisbeth Møller, Jesus Rodriguez Jorge, Marko Hawlina, Alberto Auricchio, José-Alain Sahel, Sandrine Marlin, Eberhart Zrenner, Isabelle Audo, Christine Petit,
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients,
European Journal of Human Genetics, 2016, 24 (12), pp.1730-1738. ⟨10.1038/ejhg.2016.99⟩.
2016
Paul K Potter, Michael R Bowl, Prashanthini Jeyarajan, Laura Wisby, Andrew Blease, Michelle E Goldsworthy, Michelle M Simon, Simon Greenaway, Vincent Michel, Alun Barnard, Carlos Aguilar, Thomas Agnew, Gareth Banks, Andrew Blake, Lauren Chessum, Joanne Dorning, Sara Falcone, Laurence Goosey, Shelley Harris, Andy Haynes, Ines Heise, Rosie Hillier, Tertius Hough, Angela Hoslin, Marie Hutchison, Ruairidh King, Saumya Kumar, Heena V Lad, Gemma Law, Robert E Maclaren, Susan Morse, Thomas Nicol, Andrew Parker, Karen Pickford, Siddharth Sethi, Becky Starbuck, Femke Stelma, Michael Cheeseman, Sally H Cross, Russell G Foster, Ian J Jackson, Stuart N Peirson, Rajesh V Thakker, Tonia Vincent, Cheryl Scudamore, Sara Wells, Aziz El-Amraoui, Christine Petit, Abraham Acevedo-Arozena, Patrick M Nolan, Roger Cox, Anne-Marie Mallon, Steve D M Brown,
Novel gene function revealed by mouse mutagenesis screens for models of age-related disease,
Nature Communications, 2016, 7, pp.12444. ⟨10.1038/ncomms12444⟩.
2016
Aziz El-Amraoui, Christine Petit,
Cadherins in the Auditory Sensory Organ,
Suzuki, S; Hirano, S. The Cadherin Superfamily, Springer, pp.341 - 361, 2016, 978-4-431-56033-3. ⟨10.1007/978-4-431-56033-3_13⟩.
2016
Andrea Lelli, Vincent Michel, Jacques Boutet de Monvel, Matteo Cortese, Montserrat Bosch-Grau, Asadollah Aghaie, Isabelle Perfettini, Typhaine Dupont, Paul Avan, Aziz El-Amraoui, Christine Petit,
Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth.,
Journal of Cell Biology, 2016, 212 (2), pp.231-44. ⟨10.1083/jcb.201509017⟩.
2014
P. Vincent, Y. Bouleau, S. Safieddine, Christine Petit, D. Dulon,
Exocytotic Machineries of Vestibular Type I and Cochlear Ribbon Synapses Display Similar Intrinsic Otoferlin-Dependent Ca2+ Sensitivity But a Different Coupling to Ca2+ Channels,
Journal of Neuroscience, 2014, 34 (33), pp.10853-10869. ⟨10.1523/JNEUROSCI.0947-14.2014⟩.
2014
Kazusaku Kamiya, Vincent Michel, Fabrice Giraudet, Brigitte Riederer, Isabelle Foucher, Samantha Papal, Isabelle Perfettini, Sébastien Le Gal, Elisabeth Verpy, Weiliang Xia, Ursula Seidler, Maria-Magdalena Georgescu, Paul Avan, Aziz El-Amraoui, Christine Petit,
An unusually powerful mode of low-frequency sound interference due to defective hair bundles of the auditory outer hair cells,
Proceedings of the National Academy of Sciences of the United States of America, 2014, 111 (25), pp.9307-12. ⟨10.1073/pnas.1405322111⟩.
2014
Aziz El-Amraoui, Christine Petit,
The retinal phenotype of Usher syndrome: Pathophysiological insights from animal models
Atteinte rétinienne dans le syndrome de Usher : contribution des modèles animaux à la physiopathologie,
Comptes Rendus. Biologies, 2014, 337 (3), pp.167 - 177. ⟨10.1016/j.crvi.2013.12.004⟩.
2014
Elsa Lhériteau, Lolita Petit, Michel Weber, Guylène Le Meur, Jack-Yves Deschamps, Lyse Libeau, Alexandra Mendes-Madeira, Caroline Guihal, Achille François, Richard Guyon, Nathalie Provost, Françoise Lemoine, Samantha Papal, Aziz El-Amraoui, Marie-Anne Colle, Philippe Moullier, Fabienne Rolling,
Successful Gene Therapy in the RPGRIP1-deficient Dog: a Large Model of Cone-Rod Dystrophy.,
Molecular Therapy, 2014, 22 (2), pp.265-77. ⟨10.1038/mt.2013.232⟩.
2013
Samantha Papal, Matteo Cortese, Kirian Legendre, Nasrin Sorusch, Joseph Dragavon, Iman Sahly, Spencer Shorte, Uwe Wolfrum, Christine Petit, Aziz El-Amraoui,
The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route,
Human Molecular Genetics, 2013, 22 (18), pp.3773 - 3788. ⟨10.1093/hmg/ddt228⟩.
2012
Charles-Antoine Dutertre, Sonia Amraoui, Annalisa Derosa, Jean-Pierre Jourdain, Lene Vimeux, Matthieu Goguet, Severine Degrelle, Vincent Feuillet, Anne-Sophie Liovat, Michaela Müller-Trutwin, Nipa Decroix, Christiane Deveau, Laurence Meyer, Cécile Goujard, Pierre Loulergue, Odile Launay, Yolande Richard, Anne Hosmalin,
Pivotal role of M-DC8+ monocytes from viremic HIV-infected patients in TNF overproduction in response to microbial products.,
Blood, 2012, 120 (11), pp.2259-2268. ⟨10.1182/blood-2012-03-418681⟩.
2011
Crystel Bonnet, M'Hamed Grati, Sandrine Marlin, Jacqueline Levilliers, Jean-Pierre Hardelin, Marine Parodi, Magali Niasme-Grare, Diana Zelenika, Marc Délépine, Delphine Feldmann, Laurence Jonard, Aziz El-Amraoui, Dominique Weil, Bruno Delobel, Christophe Vincent, Hélène Dollfus, Marie-Madeleine Eliot, Albert David, Catherine Calais, Jacqueline Vigneron, Bettina Montaut-Verient, Dominique Bonneau, Jacques Dubin, Christel Thauvin, Alain Duvillard, Christine Francannet, Thierry Mom, Didier Lacombe, Françoise Duriez, Valérie Drouin-Garraud, Marie-Françoise Thuillier-Obstoy, Sabine Sigaudy, Anne-Marie Frances, Patrick Collignon, Georges Challe, Rémy Couderc, Mark Lathrop, José-Alain Sahel, Jean Weissenbach, Christine Petit, Françoise Denoyelle,
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis.,
Orphanet Journal of Rare Diseases, 2011, 6 (1), pp.21. ⟨10.1186/1750-1172-6-21⟩.
2008
Kirian Legendre, Saaid Safieddine, Polonca Küssel-Andermann, Christine Petit, Aziz El-Amraoui,
αII-βV spectrin bridges the plasma membrane and cortical lattice in the lateral wall of the auditory outer hair cells,
Journal of Cell Science, 2008, 121 (20), pp.3347-3356. ⟨10.1242/jcs.028134⟩.
2008
Michel Leibovici, Saaid Safieddine, Christine Petit,
[Chapter 8] Mouse Models for Human Hereditary Deafness,
Mouse Models of Developmental Genetic Disease, 84, Elsevier, pp.385-429, 2008, Current Topics in Developmental Biology, 978-0-12-374454-8. ⟨10.1016/S0070-2153(08)00608-X⟩.
2007
Raphael Etournay, Ingrid Zwaenepoel, Isabelle Perfettini, Pierre Legrain, Christine Petit, Aziz El-Amraoui,
Shroom2, a myosin-VIIa- and actin-binding protein, directly interacts with ZO-1 at tight junctions.,
Journal of Cell Science, 2007, 120 (16), pp.2838-50. ⟨10.1242/jcs.002568⟩.
2006
Isabelle Roux, Saaid Safieddine, Régis Nouvian, M'Hamed Grati, Marie-Christine Simmler, Amel Bahloul, Isabelle Perfettini, Morgane Le Gall, Phillipe Rostaing, Ghislaine Hamard, Antoine Triller, Paul Avan, Tobias Moser, Christine Petit,
Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse.,
Cell, 2006, 127 (2), pp.277-89. ⟨10.1016/j.cell.2006.08.040⟩.
2005
Avital Adato, Gaëlle Lefèvre, Benjamin Delprat, Vincent Michel, Nicolas Michalski, Sébastien Chardenoux, Dominique Weil, Aziz El-Amraoui, Christine Petit,
Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells,
Human Molecular Genetics, 2005, 14 (24), pp.3921 - 3932. ⟨10.1093/hmg/ddi416⟩.
2005
Aziz El-Amraoui, Christine Petit,
Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells,
Journal of Cell Science, 2005, 118 (20), pp.4593-4603. ⟨10.1242/jcs.02636⟩.
2005
Aziz El-Amraoui, Gaëlle Lefèvre, Jean-Pierre Hardelin, Christine Petit,
Syndrome de Usher de type 1 et développement de la touffe ciliaire des cellules sensorielles de l’oreille interne
Usher syndrome type I and the differentiation of inner ear sensory cells’ hair bundles,
médecine/sciences, 2005, 21 (8-9), pp.737-40. ⟨10.1051/medsci/2005218-9737⟩.
2005
Raphael Etournay, Aziz El-Amraoui, Amel Bahloul, Stéphane Blanchard, Isabelle Roux, Guillaume Pézeron, Nicolas Michalski, Laurent Daviet, Jean-Pierre Hardelin, Pierre Legrain, Christine Petit,
PHR1, an integral membrane protein of the inner ear sensory cells, directly interacts with myosin 1c and myosin VIIa.,
Journal of Cell Science, 2005, 118 (13), pp.2891-99. ⟨10.1242/jcs.02424⟩.
2005
Avital Adato, Vincent Michel, Yoshiaki Kikkawa, Jan Reiners, Kumar N Alagramam, Dominique Weil, Hiromichi Yonekawa, Uwe Wolfrum, Aziz El-Amraoui, Christine Petit,
Interactions in the network of Usher syndrome type 1 proteins,
Human Molecular Genetics, 2004, 14, pp.347 - 356. ⟨10.1093/hmg/ddi031⟩.
2005
Benjamin Delprat, Vincent Michel, Richard Goodyear, Yasuhiro Yamasaki, Nicolas Michalski, Aziz El-Amraoui, Isabelle Perfettini, Pierre Legrain, Guy Richardson, Jean-Pierre Hardelin, Christine Petit,
Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly,
Human Molecular Genetics, 2004, 14 (3), pp.401 - 410. ⟨10.1093/hmg/ddi036⟩.
2004
Sandra Sousa, Didier Cabanes, Aziz El-Amraoui, Christine Petit, Marc Lecuit, Pascale Cossart,
Unconventional myosin VIIa and vezatin, two proteins crucial for Listeria entry into epithelial cells,
Journal of Cell Science, 2004, 117 (Pt 10), pp.2121-2130. ⟨10.1242/jcs.01066⟩.
2003
Claire Desnos, Jean-Sébastien Schonn, Sébastien Huet, Viet Samuel Tran, Aziz El-Amraoui, Graça Raposo, Isabelle Fanget, Catherine Chapuis, Gaël Ménasché, Geneviève de Saint Basile, Christine Petit, Sophie Cribier, Jean-Pierre Henry, François Darchen,
Rab27A and its effector MyRIP link secretory granules to F-actin and control their motion towards release sites,
Journal of Cell Biology, 2003, 163 (3), pp.559. ⟨10.1083/jcb.200302157⟩.
2003
Philomena Mburu, Mirna Mustapha, Anabel Varela, Dominique Weil, Aziz El-Amraoui, Ralph H Holme, Andreas Rump, Rachel E Hardisty, Stéphane Blanchard, Roney S Coimbra, Isabelle Perfettini, Nick Parkinson, Ann-Marie Mallon, Pete Glenister, Mike J Rogers, Adam J Paige, Lee Moir, Jo Clay, Andre Rosenthal, Xue Zhong Liu, Gonzalo Blanco, Karen P Steel, Christine Petit, Steve D M Brown,
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31,
Nature Genetics, 2003, 34, pp.421-428. ⟨10.1038/ng1208⟩.
2000
Polonca Küssel-Andermann, Aziz El-Amraoui, Saaid Safieddine, Sylvie Nouaille, Isabelle Perfettini, Marc Lecuit, Pascale Cossart, Uwe Wolfrum, Christine Petit,
Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex,
EMBO Journal, 2000, 19 (22), pp.6020-6029. ⟨10.1093/emboj/19.22.6020⟩.
2000
Polonca Küssel-Andermann, Aziz El-Amraoui, Saaid Safieddine, Jean-Pierre Hardelin, Sylvie Nouaille, Jacques Camonis, Christine Petit,
Unconventional Myosin VIIA Is a Novel A-kinase-anchoring Protein,
Journal of Biological Chemistry, 2000, 275 (38), pp.29654-29659. ⟨10.1074/jbc.M004393200⟩.
1999
Shin'Ichiro Yasunaga, M'Hamed Grati, Martine Cohen-Salmon, Aziz El-Amraoui, Mirna Mustapha, Nabiha Salem, Elie El-Zir, Jacques Loiselet, Christine Petit,
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness,
Nature Genetics, 1999, 21 (4), pp.363-369. ⟨10.1038/7693⟩.
1999
Christian Kubisch, Björn Schroeder, Thomas Friedrich, Björn Lütjohann, Aziz El-Amraoui, Sandrine Marlin, Christine Petit, Thomas Jentsch,
KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness,
Cell, 1999, 96 (3), pp.437-446. ⟨10.1016/s0092-8674(00)80556-5⟩.
1997
Iman Sahly, Aziz El-Amraoui, Marc Abitbol, Christine Petit, Jean-Louis Dufier,
Expression of myosin VIIA during mouse embryogenesis,
Anatomy and Embryology, 1997, 196 (2), pp.159-170. ⟨10.1007/s004290050088⟩.
1997
Fabien Crozet, Aziz El Amraoui, Stéphane Blanchard, Marc Lenoir, Chantal Ripoll, Philippe Vago, Christian Hamel, Cécile Fizames, Fabienne Levi-Acobas, Danièle Depétris, Marie-Genevı̀eve Mattei, Dominique Weil, Rémy Pujol, Christine Petit,
Cloning of the Genes Encoding Two Murine and Human Cochlear Unconventional Type I Myosins,
Genomics, 1997, 40 (2), pp.332-341. ⟨10.1006/geno.1996.4526⟩.
1996
Catherine Verney, Aziz El Amraoui, Nada Zecevic,
Comigration of tyrosine hydroxylase- and gonadotropin-releasing hormone-immunoreactive neurons in the nasal area of human embryos,
Developmental Brain Research, 1996, 97 (2), pp.251-259. ⟨10.1016/s0165-3806(96)00147-2⟩.
1996
A El-Amraoui, Iman Sahly, Serge Picaud, José Sahel, Marc Abitbol, Christine Petit,
Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells,
Human Molecular Genetics, 1996, 5 (8), pp.1171-1178. ⟨10.1093/hmg/5.8.1171⟩.
1996
D Weil, G Levy, I Sahly, F Levi-Acobas, S Blanchard, A El-Amraoui, F Crozet, H Philippe, M Abitbol, C Petit,
Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia.,
Proceedings of the National Academy of Sciences of the United States of America, 1996, 93 (8), pp.3232-3237. ⟨10.1073/pnas.93.8.3232⟩.